"Baylor Genetics"[submitter] AND "WASHC5-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1030375	NM_014846.4(WASHC5):c.2849A>G (p.Lys950Arg)	WASHC5, WASHC5-AS1 (K950R +1 more)	Single nucleotide variant (missense variant)	Ritscher-Schinzel syndrome 1 +1 more	GUncertain significance
Select item 1030374	NM_014846.4(WASHC5):c.2533A>G (p.Thr845Ala)	WASHC5, WASHC5-AS1 (T697A +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Hereditary spastic paraplegia 8 +2 more	GUncertain significance